HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Aminophenyl)methanesulfonamide → HCID 69267199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Aminophenyl)methanesulfonamide | HCID 10821407 | — |
| Reactant | N5-(2-Chloro-pyrimidin-4-yl)-1-ethyl-N2,N5-dimethyl-1H-benzoimidazole-2,5-diamine | HCID 59674121 | — |
| Product | HCID 69267199 | HCID 69267199 | — |
Reaction Steps
The title compound was prepared following the procedure of Example 1 with N5-(2-Chloro-pyrimidin-4-yl)-1-ethyl-N2,N5-dimethyl-1H-benzoimidazole-2,5-diamine (79 mg, 0.25 mmol) and (4-amino-phenyl)-methanesulfonamide (46 mg, 0.25 mmol) as a white solid (110 mg, 88%). 1H NMR (300 MHz, d6-DMSO) δ 9.24 (s, 1H), 7.81 (d, J=6.0 Hz, 1H), 7.74 (m, 3H), 7.36 (d, J=8.1 Hz, 1H), 7.17-7.20 (M, 3H), 6.96 (d, J=8.4 Hz, 1H), 6.78 (s, 2H), 5.70 (d, J=6.0 Hz, 1H), 4.09-4.16 (m, 4H), 3.45 (s, 3H), 2.97 (d, J=4.5 Hz, 3H), 1.24 (t, J=6.9 Hz, 3H) ppm. MS (ESI) m/z=467 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07338959B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-51a1dc2e6c9d46bdaffc7e1ff439c018 |
| Source note | uspto-grants-2008_03 |